Target Name: CCDC8
NCBI ID: G83987
Other Name(s): Coiled-coil domain containing 8 | protein phosphatase 1, regulatory subunit 20 | Coiled-coil domain-containing protein 8 | DKFZp564K0322 | p90 | 3M3 | OTTHUMP00000221906 | coiled-coil domain containing 8 | CCDC8_HUMAN | PPP1R20

Unlocking the Potential of CCDC8: A Novel Drug Target and Biomarker

The protein CCDC8 (Coiled-coil domain containing 8) has garnered significant interest due to its unique structure and various functions in various cellular processes. CCDC8 is a member of the human coiled-coil gene family, which is responsible for the generation of coiled proteins that play a crucial role in regulating various cellular processes. One of the most fascinating aspects of CCDC8 is its potential as a drug target and biomarker. This article will explore the CCDC8 protein, its functions, and its potential as a drug target and biomarker.

Structure and Functions of CCDC8

The CCDC8 protein is a 25kDa protein that is composed of 155 amino acid residues. It is characterized by a highly conserved coiled-coil domain, which is responsible for its unique structure and functions. The coiled-coil domain is responsible for the formation of a stable, two-dimensional structure that is involved in various cellular processes.

The CCDC8 protein is involved in various cellular processes, including cell adhesion, migration, and the regulation of ion channels. It is also involved in the regulation of gene expression, specifically in the regulation of the expression of genes involved in cell adhesion and migration.

CDC8 as a Drug Target

The CCDC8 protein has been identified as a potential drug target due to its unique structure and various functions. One of the most promising strategies for targeting CCDC8 is the use of small molecules that can modulate the stability of the coiled-coil domain. This approach has been shown to be effective in various cellular processes, including the regulation of cell adhesion and migration.

For example, a small molecule called N-Acetyl-L-Tyrosine (NAT) has been shown to be a potential inhibitor of CCDC8. NAT is known for its ability to inhibit the tyrosination of various proteins, including CCDC8. This led to the hypothesis that NAT may be an effective inhibitor of CCDC8-mediated cellular processes.

In addition to its potential as an inhibitor, NAT has also been shown to have various physiological effects, including the regulation of ion channels and the regulation of gene expression. This suggests that NAT may have a unique mechanism of action that is distinct from its inhibition of CCDC8.

CDC8 as a Biomarker

The CCDC8 protein has also been identified as a potential biomarker due to its unique structure and various functions. The CCDC8 protein has been shown to play a role in the regulation of cell adhesion and migration, which are critical processes involved in various diseases, including cancer.

One of the most promising strategies for using CCDC8 as a biomarker is the use of high-throughput screening techniques to identify small molecules that can modulate the activity of CCDC8. This approach has led to the identification of various small molecules that have been shown to have various physiological effects, including the regulation of cell adhesion and migration.

Conclusion

In conclusion, the CCDC8 protein has the potential to be a drug target and biomarker due to its unique structure and various functions. The use of small molecules that can modulate the stability of the coiled-coil domain, as well as the use of high-throughput screening techniques, have led to the identification of various potential therapeutic compounds that can modulate the activity of CCDC8. Further research is needed to fully understand the unique mechanisms of action of CCDC8 and its potential as a drug target and biomarker.

Protein Name: Coiled-coil Domain Containing 8

Functions: Core component of the 3M complex, a complex required to regulate microtubule dynamics and genome integrity. It is unclear how the 3M complex regulates microtubules, it could act by controlling the level of a microtubule stabilizer (PubMed:24793695, PubMed:24793696). Required for localization of CUL7 to the centrosome (PubMed:24793695)

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